ENST00000367698.4:c.873T>A
MANE Select
|
ENSP00000356671.3:p.Arg291=
|
|
ENST00000367698.3:c.873T>A
|
ENSP00000356671.3:p.Arg291=
|
|
ENST00000487183.1:n.524T>A
|
|
|
ENST00000617423.4:c.559+2032T>A
|
ENSP00000478688.1:n.559+2032T>A
|
|
NM_000488.3:c.873T>A , LRG_577t1:c.873T>A
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NP_000479.1:p.Arg291=
|
|
XM_005245198.2:c.729T>A
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XP_005245255.1:p.Arg243=
|
|
NM_001365052.1:c.729T>A
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NP_001351981.1:p.Arg243=
|
|
NM_000488.4:c.873T>A
MANE Select
|
NP_000479.1:p.Arg291=
|
|
NM_001365052.2:c.729T>A
|
NP_001351981.1:p.Arg243=
|
|
NM_001386302.1:c.996T>A
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NP_001373231.1:p.Arg332=
|
|
NM_001386303.1:c.954T>A
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NP_001373232.1:p.Arg318=
|
|
NM_001386304.1:c.852T>A
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NP_001373233.1:p.Arg284=
|
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NM_001386305.1:c.816T>A
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NP_001373234.1:p.Arg272=
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NM_001386306.1:c.657T>A
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NP_001373235.1:p.Arg219=
|
|